CFTR-NGS variants catalogue
Variant hg19:chr7:117188797A/G
Name | NM_000492.4:c.1312A>G |
Protein name | NP_000483.3:p.(Thr438Ala) |
Genomic name (hg19) | chr7:g.117188797A>G UCSC gnomAD |
#Exon/intron | exon 10 |
Legacy Name | T438A |
Type in CFTR-NGS catalogue | artefact |
Class in CFTR-France | not reported |
WT sequence | CTTCAGTAATTTCTCACTTCTTGGT A CTCCTGTCCTGAAAGATATTAATTT |
Mutant sequence | CTTCAGTAATTTCTCACTTCTTGGT G CTCCTGTCCTGAAAGATATTAATTT |
MAF (GnomAD) | 5.44e-02 |
Splicing prediction (SpliceAI) | AG: 0.00 (-31) AL: 0.00 (34) DG: 0.00 (-31) DL: 0.00 (-3) |
Not found | Not found | dbSNP rs201434579 |
Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
not present | not performed |
Color code: non disease-causing < VUS1 < VUS2 < VUS3 < VUS4 < VUS5 < disease-causing |
No patient found in CFTR-France |
TOTAL NUMBER OF INDIVIDUALS | 13 |
---|---|
Asymptomatic | 7 |
CF | 2 |
Pending (NBS) | 2 |
Suspicion of CF | 2 |
ID | Phenotype | Laboratory | Experiment | Variant status | Variant filter | Quality score | Depth of coverage |
---|---|---|---|---|---|---|---|
MUCO07300 | Asymptomatic | Montpellier | 100714_varilh | heterozygous | PASS | 211 | 102 |
MUCO07318 | Asymptomatic | Montpellier | 100714_varilh | heterozygous | PASS | 289 | 129 |
MUCO07407 | Asymptomatic | Montpellier | 100714_varilh | heterozygous | PASS | 208 | 93 |
MUCO07621 | Asymptomatic | Montpellier | 100714_varilh | heterozygous | PASS | 1393 | 172 |
9881 | Asymptomatic | Montpellier | 160218_varilh | heterozygous | LowVariantFreq | 514 | 1048 |
9004 | Asymptomatic | Montpellier | 40216_varilh | heterozygous | PASS | 1192 | 511 |
9878 | Asymptomatic | Montpellier | 160218_varilh | heterozygous | LowVariantFreq | 2368 | 1155 |
9880 | CF | Montpellier | 160218_varilh | heterozygous | LowVariantFreq | 351 | 765 |
9877 | CF | Montpellier | 160218_varilh | heterozygous | LowVariantFreq | 1469 | 1092 |
6 | Pending (NBS) | Montpellier | 150517_varilh | heterozygous | PASS | 795 | 421 |
11 | Pending (NBS) | Montpellier | 150517_varilh | heterozygous | LowVariantFreq | 1004 | 594 |
8892 | Suspicion of CF | Montpellier | 40216_varilh | heterozygous | PASS | 519 | 210 |
cad200370 | Suspicion of CF | Montpellier | 151220_Altieri | heterozygous | LowVariantFreq | 34 | 173 |